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rs397508094

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508094(-;-)
Make rs397508094(-;T)
Make rs397508094(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2445249
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508094
ClinGenrs397508094
ebirs397508094
HLIrs397508094
Exacrs397508094
Varsomers397508094
Maprs397508094
PheGenIrs397508094
hapmaprs397508094
1000 genomesrs397508094
hgdprs397508094
ensemblrs397508094
gopubmedrs397508094
geneviewrs397508094
scholarrs397508094
googlers397508094
pharmgkbrs397508094
gwascentralrs397508094
openSNPrs397508094
23andMers397508094
23andMe allrs397508094
SNP Nexus

SNPshotrs397508094
SNPdbers397508094
MSV3drs397508094
GWAS Ctlgrs397508094
Max Magnitude0
ClinVar
Risk rs397508094(T;T)
Alt rs397508094(T;T)
Reference Rs397508094(;)
Significance Untested
Disease Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype
Reversed 0
HGVS NC_000011.9:g.2466479dupT
CLNSRC ClinVar
CLNACC RCV000045991.2,